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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036256Generated: October 26, 2026

Diiodomethane → 4-(5-Fluoro-4-iodo-2-methylphenyl)-2-methylpyridine

https://huagongshe.com/reaction/1036256

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiiodomethaneHCID 6346—
ReactantIsoamyl NitriteHCID 8053—
Reactant2-Fluoro-5-methyl-4-(2-methylpyridin-4-yl)anilineHCID 58447709—
Product4-(5-Fluoro-4-iodo-2-methylphenyl)-2-methylpyridineHCID 58447915—

Reaction Conditions

Temperature100 °C

Reaction Steps

To the solution of 2-fluoro-5-methyl-4-(2-methylpyridin-4-yl)aniline 191-3 (1.02 g, 4.7 mmol) in CH2I2 (16 mL) was added isoamyl nitrite (6 mL) slowly at −10° C. After 20 minutes, the reaction was heated to 100° C. for 2 hours. The solvent was removed by rotary evaporation and the residue was dissolved in ethyl acetate and washed with Na2S2O5, brine and taken to dryness by rotary evaporation. The residue was purified by silica gel flash chromatography, eluted with 40% ethyl acetate in hexane to give 4-(5-fluoro-4-iodo-2-methylphenyl)-2-methylpyridine 191-4. MS m/z 328.10 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546396B2
Source datasetuspto-grants-2013_10
ORD IDord-56d2f48eed5e4bf180414012be71f931
Source noteuspto-grants-2013_10